The CORE-MD Consortium has organised it’s eighth webinar for Tuesday 05 of December. The title of this webinar is “IT tools for regulatory science: aggregating available data for assisting Expert Panels and improving post-market surveillance“
Moderator: Prof. Alan Fraser
The Webinar will address the following topics:
- 17.00 – 17.05 | Introduction by Moderator, Prof. Alan Fraser, BioMed Alliance, Scientific Coordinator of CORE-MD.
- 17.05 – 17.25 | Exploiting IT tools to retrieve alerts and reports of high-risk medical devices – Prof. Enrico Caiani, Politecnico Di Milano.
- 17.25 – 17.35 | The EMA’s expert panels role in Surveillance – Dr. Miguel Antunes, EMA Expert panel secretariat & Prof. Rob Nelissen, Expert Panel’s Member.
- 17.35 – 17.45 | Post-market surveillance and real-world evidence – Mr. Sanjeev Yoganathan, Scientific Officer, MSc Health Informatics.
- 17.45 – 17.50 | Discussant – Dr Paul Piscoi, European Commission, DG Santé, Medical Devices Unit.
- 17.50 – 18.15 | Q&A from the audience.
Learning Objectives:
- To discover the activities performed during the CORE-MD project in support to automated data
aggregation of safety notices for post-market surveillance. - To understand EMA Expert Panel’s roles in post-market surveillance and vigilance.
- To receive regulator’s perspective on the use of real-world evidence.
